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1.
Acta Gastroenterol Latinoam ; 31(1): 27-30, 2001 Mar.
Artigo em Espanhol | MEDLINE | ID: mdl-11370177

RESUMO

We present a case of Idiopathic Portal Hypertension (IPH) with Splenic infarct in a 23-year-old female. She was referred to the hospital because of enlargement of liver and spleen. A computed axial tomography revealed Splenic infarct. The spleen was surgically removed. At laparotomy the liver was found to be enlarged and a liver biopsy performed. The biopsy showed characteristic changes of IPH. After the splenic resection all hematologic manifestations disappeared, suggesting that they were due to hypersplenism. The IPH is very uncommon in western countries. We don't know of any case previously reported in Argentina and our patient is the first case of IPH with Splenic infarct.


Assuntos
Hipertensão Portal/complicações , Infarto do Baço/etiologia , Adulto , Biópsia , Feminino , Humanos , Hipertensão Portal/patologia , Infarto do Baço/patologia , Esplenomegalia/complicações , Tomografia Computadorizada por Raios X
2.
Acta gastroenterol. latinoam ; Acta gastroenterol. latinoam;31(1): 27-30, 2001 Mar.
Artigo em Espanhol | BINACIS | ID: bin-39554

RESUMO

We present a case of Idiopathic Portal Hypertension (IPH) with Splenic infarct in a 23-year-old female. She was referred to the hospital because of enlargement of liver and spleen. A computed axial tomography revealed Splenic infarct. The spleen was surgically removed. At laparotomy the liver was found to be enlarged and a liver biopsy performed. The biopsy showed characteristic changes of IPH. After the splenic resection all hematologic manifestations disappeared, suggesting that they were due to hypersplenism. The IPH is very uncommon in western countries. We dont know of any case previously reported in Argentina and our patient is the first case of IPH with Splenic infarct.

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